Assistant Manager Clinical Research (Hybrid) - Radiology
Quick Summary
Provides leadership and oversight to our research programs. Will oversee all IRB, RDRC, and FDA submissions. Serves as a resource to provide comprehensive information to clinical research staff.
Bachelor’s degree or combination of education and/or experience may substitute for minimum education. Certifications/Professional Licenses:The list below may include all acceptable certifications,
Responsibilities
~2 min read- →Provides leadership and oversight to our research programs.
- →Will oversee all IRB, RDRC, and FDA submissions.
- →Serves as a resource to provide comprehensive information to clinical research staff.
- →May perform duties inclusive of those delegated to a Clinical Research Coordinator III and/or Clinical Research Supervisor.
- →Assists in the management of the day-to-day functions of the research team.
- →Utilizes critical thinking in the management of clinical trials.
- →Develops and implements policies and procedures.
- →Provides comprehensive direction to clinical research personnel.
- →Supervises research team, including hiring, terminating, and scheduling assignments to personnel; provides performance feedback/annual reviews.
- →Onboards, educates, and trains new staff; serves as a point of reference for current research staff.
- →Identifies problems and/or inconsistencies with personnel and study conduct and develops and implements corrective action plans.
- →Provides higher level oversight and management of all phases of study/protocol lifecycle.
- →May assist in the strategic planning of clinical research, including evaluation of the research team’s bandwidth for new trials and assessment of new protocols and subsequent assignment of the protocol to research staff.
- →May order supplies needed for the research projects and research group.
- →May assist in monitoring ongoing financial state, patient recruitment milestones, and personnel resources necessary to conduct the research. May assist financial and grant administrators with federal and sponsor funded trials.
- →Researches and recommends new methods and procedures to maintain standards and improve quality.
- →Performs other duties incidental to the work described above.
Job Location/Working Conditions
- Normal office environment.
- Exposure to blood-borne pathogens.
- Patient care setting.
- Ability to travel to various on- and off-campus locations.
Physical Effort
- Typically sitting at a desk or table.
- Typically standing or walking.
- Typically bending, crouching, stooping.
- Occasional lifting (25 lbs or less).
Equipment
- Office equipment.
- Lab/research equipment.
- Clinical/diagnostic equipment.
Requirements
~1 min read- Phlebotomy experience/certification.
- SOCRA/ACRP certified.
- Familiarity with University systems.
- Effective working knowledge of investigator initiated, industry sponsored, and NIH funded multi-center trials of all phases.
- Knowledge of grant compliance and FDA regulations.
About the Role
~1 min readFor frequently asked questions about the application process, please refer to our External Applicant FAQ.
If you are unable to use our online application system and would like an accommodation, please email CandidateQuestions@wustl.edu or call the dedicated accommodation inquiry number at 314-935-1149 and leave a voicemail with the nature of your request.
All qualified individuals must be able to perform the essential functions of the position satisfactorily and, if requested, reasonable accommodations will be made to enable employees with disabilities to perform the essential functions of their job, absent undue hardship.What We Offer
~1 min readPersonal
Location & Eligibility
About this job
- Posted
- 19 days ago
Listing Details
- Posted
- September 25, 2026
- First seen
- October 11, 2026
- Last seen
- October 13, 2026
Posting Health
- Days active
- 2
- Repost count
- 0
- Trust Level
- 19%
- Scored at
- October 14, 2026
Signal breakdown
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